Linked Data
dbSNP Id:
rs1006583803
gnomAD v2:
6-139693937-T-C
gnomAD v3:
6-139372800-T-C
gnomAD v4:
6-139372800-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.139372800T>C , CM000668.2:g.139372800T>C | GRCh38 |
| NC_000006.11:g.139693937T>C , CM000668.1:g.139693937T>C | GRCh37 |
| NC_000006.10:g.139735630T>C | NCBI36 |
| NG_016169.1:g.6849A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367651.4:c.*332A>G MANE Select | ENSP00000356623.2:n.*332A>G | |
| ENST00000367651.3:c.*332A>G | ENSP00000356623.2:n.*332A>G | |
| ENST00000536159.2:c.*332A>G | ENSP00000442831.1:n.*332A>G | |
| ENST00000537332.2:c.*332A>G | ENSP00000444198.2:n.*332A>G | |
| NM_001168388.2:c.*332A>G | NP_001161860.1:n.*332A>G | |
| NM_001168389.2:c.*332A>G | NP_001161861.2:n.*332A>G | |
| NM_006079.4:c.*332A>G | NP_006070.2:n.*332A>G | |
| NM_006079.5:c.*332A>G MANE Select | NP_006070.2:n.*332A>G | |
| NM_001168388.3:c.*332A>G | NP_001161860.1:n.*332A>G | |
| NM_001168389.3:c.*332A>G | NP_001161861.2:n.*332A>G |